K232417
- 510(k) number
- K232417
- Device name
- MR Q; MR Q SUPINE; MR Q SLT
- Applicant
- Meridian AG CH
- Product code
- HQF — Laser, Ophthalmic
- Decision date
- 2024-01-25
- Date received
- 2023-08-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K232417
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.